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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198845Generated: October 26, 2026

1-Naphthol → 1-(alpha-Naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane

https://huagongshe.com/reaction/2198845

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphtholHCID 7005—
ReactantSodium HydroxideHCID 14798—
Reactant1-(Iso-propyl)-3-benzyloxyazetidineHCID 20517324—
SolventDiethyl EtherHCID 3283—
Product1-(alpha-Naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propaneHCID 1305570879%

Reaction Conditions

Temperature200 °C

Reaction Steps

To a mixture of 6.2 parts of 1-(iso-propyl)-3-benzyloxyazetidine and 43 parts of α-naphthol 1.5 parts of sodium hydroxide was added, and the mixture was heated at 200° C. for 16 hours. The reaction mixture was cooled, and 100 parts of ether were added thereto. Excessive α-naphthol was removed by extraction with 2 N-sodium hydroxide aqueous solution. The remaining ether layer was washed in water and dried over anhydrous sodium sulfate. After distillation of ether, the residue was subjected to distillation to yield 8.3 parts of 1-(α-naphthoxy)-2-benzyloxy-3-(iso-propylamino)-propane boiling at 192°-195° C. The yield was 79%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04360464
Source datasetuspto-grants-1982_11
ORD IDord-a58a529d3dcc43d5b190b38142ae8bec
Source noteuspto-grants-1982_11